Secondary Hemostasis

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Last updated 11:19 PM on 9/17/26
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15 Terms

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Substrate

The main reactant is fibrinogen

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Cofactors in Secondary Hemostasis

Proteins that accelerate enzymatic reactions

  • Factor V

  • Factor VIII


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Enzymes in Secondary Hemostasis

Two types

  • Transaminase that cross-linked the fibrin: factor XIII

  • Serine proteases that cleave peptide bond: The other factors


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Contact Group Factors {Properties}

Contact activation and initiate intrinsic pathway

  • Factor XII, prekallikrein (PK), high molecular weight kininogen (HMWK)

  • Not consumed during coagulation

  • Not vitamin-K dependent

  • Present in serum


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Prothrombin Group Factors {Properties}

Generating & amplifying coagulation

  • Factor II, factor VII, factor IX, factor X

  • Not consumed (except factor II)

  • Vitamin-K dependent

  • Present in serum

  • Adsorbed by BaSO4


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Thrombin-Sensitive Group {Properties}

Involved in fibrin formation & clot stabilization

  • Factor I, Factor V, Factor VIII, Factor XIII

  • Consumed during coagulation

  • Not vitamin-K dependent

  • Absent/markedly reduced in serum


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Labile Factors

Easily inactivated

  • Factor V

  • Factor VIII


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Intrinsic Factors

  • Factors XII, XI, IX, VIII

  • Test by aPTT


<ul><li><p>Factors XII, XI, IX, VIII</p></li><li><p>Test by aPTT</p></li></ul><p></p>
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Extrinsic Factors

  • Tissue thromboplastin (TF III), Factor VII

  • Test by PT


<ul><li><p>Tissue thromboplastin (TF III), Factor VII </p></li><li><p>Test by PT </p></li></ul><p></p>
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Common Pathway

  • Factors X, V, II, I, XIII

  • Test by both aPTT and PT


<ul><li><p>Factors X, V, II, I, XIII</p></li><li><p>Test by both aPTT and PT</p></li></ul><p></p>
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Intrinsic Tenase Complex

  • IXa + VIIIa + Ca2+ + phospholipid surface

  • Cleave X → Xa


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Prothrombinase Complex

  • Xa + V + Ca2+ + phospholipid surface

  • Cleave prothrombin (II) → thrombin (IIa)


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Extrinsic Tenase Complex

  • TF III + VIIa + Ca2+

  • Cleave X → Xa


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Thrombin Functions

  • Forms fibrin

  • Activates platelets

  • Amplifies the cascade by activating factor V, factor VIII, XI

  • Stabilizes clot by activating factor XIII


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Fibrin Polymerization

  • fibrin monomer combines with fibrinopeptides A & B to form weak fibrin polymer

  • Factor XIIIa and calcium cross-link fibrin polymer via covalent bond to form stable fibrin clot